scholarly journals Role of COUP-TFI during retinoic acid-induced differentiation of P19 cells to endodermal cells

2012 ◽  
Vol 228 (4) ◽  
pp. 791-800 ◽  
Author(s):  
Brandy S. Pickens ◽  
Bryan W. Teets ◽  
Kenneth J. Soprano ◽  
Dianne Robert Soprano
Keyword(s):  
Retinoic Acid ◽  
P19 Cells ◽  
Induced Differentiation ◽  
Endodermal Cells

scholarly journals Evidence for a dynamic role of the linker histone variant H1x during retinoic acid-induced differentiation of NT2 cells

FEBS Letters ◽  
2010 ◽  
Vol 584 (22) ◽  
pp. 4661-4664 ◽  
Author(s):  
Maryam Shahhoseini ◽  
Raha Favaedi ◽  
Hossein Baharvand ◽  
Vikram Sharma ◽  
Hendrik G Stunnenberg
Keyword(s):  
Retinoic Acid ◽  
Linker Histone ◽  
Histone Variant ◽  
Induced Differentiation ◽  
Nt2 Cells

scholarly journals Deletion of the Prdm3 Gene Causes a Neuronal Differentiation Deficiency in P19 Cells

2020 ◽  
Vol 21 (19) ◽  
pp. 7192
Author(s):  
Paweł Leszczyński ◽  
Magdalena Śmiech ◽  
Aamir Salam Teeli ◽  
Effi Haque ◽  
Robert Viger ◽  
...  
Keyword(s):  
Retinoic Acid ◽  
Mrna Expression ◽  
Neuronal Differentiation ◽  
Regulatory Mechanism ◽  
Gene Knockout ◽  
Luciferase Reporter ◽  
P19 Cells ◽  
Binding Factor ◽  
Domain I

PRDM (PRDI-BF1 (positive regulatory domain I-binding factor 1) and RIZ1 (retinoblastoma protein-interacting zinc finger gene 1) homologous domain-containing) transcription factors are a group of proteins that have a significant impact on organ development. In our study, we assessed the role of Prdm3 in neurogenesis and the mechanisms regulating its expression. We found that Prdm3 mRNA expression was induced during neurogenesis and that Prdm3 gene knockout caused premature neuronal differentiation of the P19 cells and enhanced the growth of non-neuronal cells. Interestingly, we found that Gata6 expression was also significantly upregulated during neurogenesis. We further studied the regulatory mechanism of Prdm3 expression. To determine the role of GATA6 in the regulation of Prdm3 mRNA expression, we used a luciferase-based reporter assay and found that Gata6 overexpression significantly increased the activity of the Prdm3 promoter. Finally, the combination of retinoic acid receptors α and β, along with Gata6 overexpression, further increased the activity of the luciferase reporter. Taken together, our results suggest that in the P19 cells, PRDM3 contributed to neurogenesis and its expression was stimulated by the synergism between GATA6 and the retinoic acid signaling pathway.

Gene Expression Analysis of Bexarotene Differentiated Acute Myeloid Leukemias Identifies Known and Novel Gene Targets.

Blood ◽  
2008 ◽  
Vol 112 (11) ◽  
pp. 1199-1199
Author(s):  
Patricia Vanessa Sanchez ◽  
Reid P Bissonnette ◽  
Donald E Tsai ◽  
Martin Carroll
Keyword(s):  
Transcription Factor ◽  
Retinoic Acid ◽  
Cell Differentiation ◽  
Cell Lines ◽  
Leukemic Cell ◽  
Myeloid Differentiation ◽  
Induced Differentiation ◽  
Pparγ Agonist ◽  
Acute Myeloid

Abstract Despite advances in understanding the molecular pathogenesis of acute myeloid leukemia (AML), therapy for relapsed disease remains inadequate with high mortalities. Clinicians at the University of Pennsylvania have demonstrated that the FDA approved retinoid X receptor (RXR) agonist bexarotene (Targretin™) stimulates leukemic cell differentiation in a subset patents with relapsed AML leading to clinical responses. This underscores the importance of identifying the mechanism by which bexarotene induces differentiation in AML in order to enhance the efficacy of this therapeutic approach. To understand the role of bexarotene and RXR receptors in leukemic cell differentiation, we initially utilized a pharmacogenetic approach to study the effects of bexarotene on AML cell lines using combinations of bexarotene with other differentiation induction agents. These studies demonstrate that bexarotene induces myeloid differentiation in MOLM14, HL60, THP-1, and NB4 cell lines but not in the myeloblastic cell line KG1a. Combination treatment of AML cell lines with bexarotene in combination with all trans retinoic acid (ATRA) enhanced differentiation suggesting that the mechanism of action for bexarotene is through RARα (retinoic acid receptor)/RXRα heterodimer stimulation. Consistent with this, differentiation induced by the drug combination was effectively blocked by the RAR antagonist, LG100815 and partially blocked by the RXR antagonist, LG101208. In contrast, bexarotene does not cooperate with valproic acid, theophylline, the PPARγ agonist rosiglitazone, or the LXR agonist T0901317. Preliminary data from quantitative RT-PCR and Affymetrix microarray analysis of bexarotene responsive AML cell lines at 3, 6, 12, and 96 hours post treatment has identified a subset of genes potentially regulated by bexarotene. CEBPε, a transcription factor known to play a critical role in granulopoiesis and PIM-1, a known oncogenic transcription factor, were among the genes that were significantly upregulated after bexarotene treatment of AML cells. Analysis of the functional role of C/EBPε in retinoid induced differentiation will be presented. Overall, this data supports the hypothesis that bexarotene, like ATRA, induces myeloid differentiation through activation of a RAR/RXR heterodimeric partner. However, other data suggests the presence of RAR independent pathways of signaling. LG100268, a pure RXR agonist induced myeloid differentiaton although not as robustly as bexarotene. Analysis of RAR and RXR mRNA expression in AML cell lines demonstrates that bexarotene does not induce expression of RARβ or p21, known targets induced by ATRA during myeloid differentiation. Chromatin immunoprecipitation assays demonstrate RXRα occupancy at RARβ and p21 promoter regions containing retinoid response elements (RARE). However, expression of these genes does not correlate with bexarotene-induced differentiation. This data suggests that although their expression has been linked to ATRA responsiveness, induction of RARβ and p21 expression is not necessary for retinoid induced myeloid differentiation. In summary, bexarotene induces myeloid differentiation through RAR dependent and independent pathways. Further analysis of the signaling events necessary for induction of myeloid differentiation by bexarotene may allow for improved selection of patients with AML who will respond to bexarotene.

Neuroblastoma Cell Response to Oxidative Stress Is Impaired by Retinoic Acid-Induced Differentiation: Role of HO-1

2016 ◽  
Vol 100 ◽  
pp. S106-S107 ◽  
Author(s):  
Mariapaola Nitti ◽  
Sabrina Piras ◽  
Anna Lisa Furfaro ◽  
Lorenzo Brondolo ◽  
Umberto Maria Marinari ◽  
...  
Keyword(s):  
Oxidative Stress ◽  
Retinoic Acid ◽  
Cell Response ◽  
Neuroblastoma Cell ◽  
Induced Differentiation

scholarly journals Role of Collagen in Retinoic Acid-induced Differentiation and Down-regulation of TGF-.BETA. Receptors in Rat Preosteoblastic RCT-1 Cells.

1997 ◽  
Vol 44 (3) ◽  
pp. 375-381 ◽  
Author(s):  
YOSHIAKI KODAMA ◽  
YASUHIRO TAKEUCHI ◽  
TOMOKO KIKUCHI ◽  
TAKAHIDE KUROKAWA ◽  
TOSHIRO FUJITA ◽  
...  
Keyword(s):  
Retinoic Acid ◽  
Tgf Beta ◽  
Down Regulation ◽  
Induced Differentiation ◽  
Beta Receptors

Role of Acetylated p53 in Regulating the Expression of map2 in Retinoic Acid-induced P19 Cells

2010 ◽  
Vol 25 (2) ◽  
pp. 71-75 ◽  
Author(s):  
Li Zhang ◽  
Li Yan ◽  
Ye Zhang ◽  
Ning-hua Wu ◽  
Yu-fei Shen
Keyword(s):  
Retinoic Acid ◽  
P19 Cells
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